We Are Teva We re Teva a leading innovative biopharmaceutical company enabled by a world-class generics business Whether it s innovating in the fields of neuroscience and immunology or delivering high-quality medicine worldwide we re dedicated to addressing patients needs now and in the future Here you will be part of a high-performing inclusive culture that values fresh thinking and collaboration You ll have the room to grow the flexibility to balance life with work and the opportunity to better health worldwide together How you ll spend your day Receipt registration and upkeep of samples in the laboratory Review of analytical data Preparation and review of analytical protocols reports Online monitoring of trends and analytical results of all applicable products Data compilation Calculation Documentation and general upkeep of Action Alert Limits Review and submission of Annual Product Review APR documents to QA Department Upkeep and Maintenance of incubators walk in chambers refrigerators stability area and Stability Chambers Intimation of field alert report to QA Identification tracking and Co-ordination of all stability batches packed at Goa site and at other approved packing site Sending samples to external laboratories for testing Provide technical guidance to team members Adherence to committed timelines to achieve Cycle Time CT target Define the analytical strategy to develop verify validate or transfer of analytical methods for new and ongoing projects Ensure maintenance upkeep and inventory of spares accessories columns glassware chemicals standards narcotic substances placebos and impurities Responsible for regulatory compliance Handling of instrument equipment breakdowns Co-ordination with service providers for instrument related services Review and Monitoring of preventive maintenance performance verification calibration of instruments equipment s Responsible for creation verification and review of non-computerized and computerized systems in Laboratory Review of analytical data generated by various analytical methods techniques in view of data integrity and Audit trails Approval of Analytical reports subject to FDA approval Timely evaluation of Pharmacopeia changes and implementation of the same Ensure timely qualification of in-house standards Responsible for reporting and investigation of Analytical Errors Out of Action Alert Limits Deviations and LIR If any Ensure CAPA closeout and effectiveness check Responsible for trackwise Ample Logic and Glorya EDMS related activities Responsible for SAP related Activities To ensure compliance to the policy and procedures requirements on Data Integrity Review of Microbiological data Ensure timely completion of assigned trainings To maintain Good Laboratory Practices To maintain the laboratory cleanliness and continuous monitoring Ensure maintenance of logbooks and all relevant registers in the laboratory Routine troubleshooting during analysis To involve in OpEx initiatives To impart awareness and refresher training To maintain cross functional and cross departmental communications Your experience and qualifications 10 Years of experience M Sc M Pharm How We ll Take Care of You At Teva better health starts from within and that includes you From day one you ll be supported with advantages designed to help you thrive in and out of work This includes generous annual leave reward plans flexible working schedules dependent on role access to tailored health support and meaningful ways to give back to the community When it comes to your career you ll be encouraged to explore evolve and shape your path Twist our one-stop shop for career development platform gives you access to a wide range of possibilities from learning programs and short-term projects to opportunities for internal growth Here you ll be part of a culture that empowers you to reach your goals and prioritize your wellbeing every step of the way Teva s Equal Employment Opportunity Commitment Teva Pharmaceuticals is committed to equal opportunity in employment It is Teva s global policy that equal employment opportunity be provided without regard to age race creed color religion sex disability pregnancy medical condition sexual orientation gender identity or expression ancestry veteran status national or ethnic origin or any other legally recognized status entitled to protection under applicable laws We are committed to a diverse and inclusive workplace for all If you are contacted for a job opportunity please advise us of any accommodations needed to support you throughout the recruitment and selection process All accommodation information provided will be treated as confidential and used only for the purpose of providing an accessible candidate experience

📌 Quality Control Analyst Ii (Goa)
🏢 Teva Pharmaceuticals
📍 Goa